DIASONICS, BERGER STEREOTACTIC NEOROBIOPSY

DIASONICS, BERGER STEREOTACTIC NEOROBIOPSY is an FDA 510(k)-cleared medical device (K851973) manufactured by Diasonics, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 25, 1985. Regulation: 8.